作者:Pilar Goya、Ana Martínez
DOI:10.1002/ardp.19883210213
日期:——
Imidazo[4,5‐c][1,2,6]thiadiazine ribosides have been prepared from furazano[3,4‐c][1,2,6]thiadiazine 5,5‐dioxides in a reaction sequence which involves introduction of the glycosidic rest, reductive cleavage of the furazan ring and cyclization. The ribosides were screened against HeLa cell cultures but showed no significant activity.
咪唑 [4,5 - c] [1,2,6] 噻二嗪核糖苷已从呋喃唑 [3,4 - c] [1,2,6] 噻二嗪 5,5 - 二氧化物在一个反应序列中制备,该反应序列涉及引入糖苷休息,呋喃环的还原裂解和环化。核苷针对 HeLa 细胞培养物进行了筛选,但没有显示出显着的活性。